CZ300329B6 - Herbicidní prostredek, zpusob hubení škodlivých rostlin a použití tohoto prostredku - Google Patents

Herbicidní prostredek, zpusob hubení škodlivých rostlin a použití tohoto prostredku Download PDF

Info

Publication number: CZ300329B6
Authority: CZ; Czechia
Prior art keywords: carbon atoms; group; compounds; denotes; alkyl
Prior art date: 1999-10-26

Application number

CZ20021461A

Other languages

Czech (cs)

English (en)

Other versions

CZ20021461A3 (cs

Inventor

Krähmer@Hansjörg

Auler@Thomas

Rosinger@Christopher

Hagemeister@Heinz

Drexler@David

Original Assignee

Bayer Cropscience Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1999-10-26

Filing date

2000-10-10

Publication date

2009-04-22

2000-10-10 Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag

2002-09-11 Publication of CZ20021461A3 publication Critical patent/CZ20021461A3/cs

2009-04-22 Publication of CZ300329B6 publication Critical patent/CZ300329B6/cs

Links

230000009931 harmful effect Effects 0.000 title claims abstract description 23
238000000034 method Methods 0.000 title claims abstract description 20
239000004009 herbicide Substances 0.000 title abstract description 23
239000003795 chemical substances by application Substances 0.000 title description 4
150000003839 salts Chemical class 0.000 claims abstract description 27
229940100389 Sulfonylurea Drugs 0.000 claims abstract description 11
239000000203 mixture Substances 0.000 claims description 79
150000001875 compounds Chemical class 0.000 claims description 60
230000002363 herbicidal effect Effects 0.000 claims description 60
125000004432 carbon atom Chemical group C* 0.000 claims description 48
235000015112 vegetable and seed oil Nutrition 0.000 claims description 37
239000008158 vegetable oil Substances 0.000 claims description 37
125000000217 alkyl group Chemical group 0.000 claims description 23
238000009472 formulation Methods 0.000 claims description 19
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
125000003545 alkoxy group Chemical group 0.000 claims description 15
239000013543 active substance Substances 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 9
239000000654 additive Substances 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
229910052757 nitrogen Inorganic materials 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
125000005133 alkynyloxy group Chemical group 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
241001611408 Nebo Species 0.000 claims 1
239000003905 agrochemical Substances 0.000 claims 1
239000010773 plant oil Substances 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 57
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230000000694 effects Effects 0.000 description 25
239000004480 active ingredient Substances 0.000 description 17
239000002253 acid Substances 0.000 description 14
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235000014113 dietary fatty acids Nutrition 0.000 description 11
239000000194 fatty acid Substances 0.000 description 11
229930195729 fatty acid Natural products 0.000 description 11
238000002360 preparation method Methods 0.000 description 10
ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 description 9
244000038559 crop plants Species 0.000 description 9
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150000004665 fatty acids Chemical class 0.000 description 8
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230000006378 damage Effects 0.000 description 7
125000004494 ethyl ester group Chemical group 0.000 description 7
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239000012141 concentrate Substances 0.000 description 6
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 6
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239000004094 surface-active agent Substances 0.000 description 6
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150000007513 acids Chemical class 0.000 description 5
239000000969 carrier Substances 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
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150000004702 methyl esters Chemical class 0.000 description 5
235000009566 rice Nutrition 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
239000011734 sodium Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
230000002195 synergetic effect Effects 0.000 description 5
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
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JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
150000002334 glycols Chemical class 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
239000007788 liquid Substances 0.000 description 4
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SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 4
238000009331 sowing Methods 0.000 description 4
239000000080 wetting agent Substances 0.000 description 4
JAXUXISKXAOIDD-UHFFFAOYSA-N 2-(5-chloroquinolin-8-yl)oxypropanedioic acid Chemical compound C1=CN=C2C(OC(C(=O)O)C(O)=O)=CC=C(Cl)C2=C1 JAXUXISKXAOIDD-UHFFFAOYSA-N 0.000 description 3
NOBPWDYRGXWVRL-UHFFFAOYSA-N 5-[(2,4-dichlorophenyl)methyl]-4,5-dihydro-1,2-oxazole-3-carboxylic acid Chemical compound C1C(C(=O)O)=NOC1CC1=CC=C(Cl)C=C1Cl NOBPWDYRGXWVRL-UHFFFAOYSA-N 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
235000021314 Palmitic acid Nutrition 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
125000005907 alkyl ester group Chemical group 0.000 description 3
125000004390 alkyl sulfonyl group Chemical group 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
239000003337 fertilizer Substances 0.000 description 3
230000012010 growth Effects 0.000 description 3
NDQZMBNEHYSVPL-UHFFFAOYSA-N methyl 2-(5-chloroquinolin-8-yl)oxyacetate Chemical compound C1=CN=C2C(OCC(=O)OC)=CC=C(Cl)C2=C1 NDQZMBNEHYSVPL-UHFFFAOYSA-N 0.000 description 3
238000002156 mixing Methods 0.000 description 3
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 3
150000007524 organic acids Chemical group 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000002689 soil Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
125000006700 (C1-C6) alkylthio group Chemical group 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
MQPLQJSDTDAHBC-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-propan-2-ylpyrazole-3-carboxylic acid Chemical compound CC(C)C1=CC(C(O)=O)=NN1C1=CC=C(Cl)C=C1Cl MQPLQJSDTDAHBC-UHFFFAOYSA-N 0.000 description 2
239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 2
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 2
WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 2
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
VRODIKIAQUNGJI-UHFFFAOYSA-N 5-phenyl-4,5-dihydro-1,2-oxazole-3-carboxylic acid Chemical compound C1C(C(=O)O)=NOC1C1=CC=CC=C1 VRODIKIAQUNGJI-UHFFFAOYSA-N 0.000 description 2
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
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241000219312 Chenopodium Species 0.000 description 2
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239000005504 Dicamba Substances 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
239000005639 Lauric acid Substances 0.000 description 2
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
239000005574 MCPA Substances 0.000 description 2
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239000005586 Nicosulfuron Substances 0.000 description 2
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229910052783 alkali metal Inorganic materials 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
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150000001342 alkaline earth metals Chemical class 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
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DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
235000020661 alpha-linolenic acid Nutrition 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
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238000006243 chemical reaction Methods 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 2
LPVVTHQFIVXMEZ-UHFFFAOYSA-N diethyl 2-(5-chloroquinolin-8-yl)oxypropanedioate Chemical compound C1=CN=C2C(OC(C(=O)OCC)C(=O)OCC)=CC=C(Cl)C2=C1 LPVVTHQFIVXMEZ-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
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150000002170 ethers Chemical class 0.000 description 2
JEMXUSHXYOXNFL-UHFFFAOYSA-N ethyl 2-(5-chloroquinolin-8-yl)oxyacetate Chemical compound C1=CN=C2C(OCC(=O)OCC)=CC=C(Cl)C2=C1 JEMXUSHXYOXNFL-UHFFFAOYSA-N 0.000 description 2
REVLCBCMFHHOGK-UHFFFAOYSA-N ethyl 4,5-dihydro-1,2-oxazole-3-carboxylate Chemical compound CCOC(=O)C1=NOCC1 REVLCBCMFHHOGK-UHFFFAOYSA-N 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
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125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 description 2
235000020778 linoleic acid Nutrition 0.000 description 2
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235000009973 maize Nutrition 0.000 description 2
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239000002480 mineral oil Substances 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
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230000003287 optical effect Effects 0.000 description 2
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125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
KBIYESXVNVTIFG-UHFFFAOYSA-N 1-[2-(1-methylcyclohexa-2,4-dien-1-yl)ethyl]-3-(4-methylphenyl)urea Chemical compound C1=CC(C)=CC=C1NC(=O)NCCC1(C)C=CC=CC1 KBIYESXVNVTIFG-UHFFFAOYSA-N 0.000 description 1
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239000004808 2-ethylhexylester Substances 0.000 description 1
ICBQXEWYZVQCFH-UHFFFAOYSA-N 3-(4-bromoanilino)-n,n-dimethylpropanamide Chemical compound CN(C)C(=O)CCNC1=CC=C(Br)C=C1 ICBQXEWYZVQCFH-UHFFFAOYSA-N 0.000 description 1
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CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
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DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
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125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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WPMLUBKROSECCN-UHFFFAOYSA-N sodium;benzenesulfonamide Chemical compound [Na+].NS(=O)(=O)C1=CC=CC=C1 WPMLUBKROSECCN-UHFFFAOYSA-N 0.000 description 1
PTMQOXHDUDYMHB-UHFFFAOYSA-N sodium;benzenesulfonylazanide Chemical compound [Na+].[NH-]S(=O)(=O)C1=CC=CC=C1 PTMQOXHDUDYMHB-UHFFFAOYSA-N 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
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YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
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ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
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YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
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Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

CZ20021461A 1999-10-26 2000-10-10 Herbicidní prostredek, zpusob hubení škodlivých rostlin a použití tohoto prostredku CZ300329B6 (cs)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19951426		1999-10-26

Publications (2)

Publication Number	Publication Date
CZ20021461A3 CZ20021461A3 (cs)	2002-09-11
CZ300329B6 true CZ300329B6 (cs)	2009-04-22

Family

ID=7926848

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CZ20021461A CZ300329B6 (cs)	1999-10-26	2000-10-10	Herbicidní prostredek, zpusob hubení škodlivých rostlin a použití tohoto prostredku

Country Status (28)

Country	Link
US (1)	US6569805B1 (fr)
EP (1)	EP1227724B1 (fr)
JP (1)	JP2003512398A (fr)
CN (1)	CN1201658C (fr)
AR (1)	AR026224A1 (fr)
AT (1)	ATE264057T1 (fr)
AU (1)	AU770910B2 (fr)
BR (1)	BR0015018A (fr)
CA (1)	CA2388909C (fr)
CL (1)	CL2004001106A1 (fr)
CO (1)	CO5231160A1 (fr)
CZ (1)	CZ300329B6 (fr)
DE (1)	DE50006096D1 (fr)
DK (1)	DK1227724T3 (fr)
ES (1)	ES2219404T3 (fr)
HR (1)	HRP20020355B1 (fr)
HU (1)	HU226076B1 (fr)
MX (1)	MXPA02004150A (fr)
MY (1)	MY120861A (fr)
PL (1)	PL200935B1 (fr)
PT (1)	PT1227724E (fr)
RS (1)	RS50472B (fr)
RU (1)	RU2266647C2 (fr)
SK (1)	SK286660B6 (fr)
TW (1)	TWI243018B (fr)
UA (1)	UA72940C2 (fr)
WO (1)	WO2001030155A2 (fr)
ZA (1)	ZA200203207B (fr)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4440354A1 (de) *	1994-11-11	1996-05-15	Hoechst Schering Agrevo Gmbh	Kombinationen aus Phenylsulfonylharnstoff-Herbiziden und Safenern
SE9801288D0 (sv) *	1998-04-14	1998-04-14	Astra Ab	Vaccine delivery system and metod of production
JP2000321600A (ja) *	1999-05-13	2000-11-24	Internatl Business Mach Corp <Ibm>	液晶表示装置及びこれの製造方法
DE10108472A1 (de) *	2001-02-22	2002-09-05	Aventis Cropscience Gmbh	Agrochemische Formulierungen
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- 2000-10-10 EP EP00967851A patent/EP1227724B1/fr not_active Expired - Lifetime
- 2000-10-10 PT PT00967851T patent/PT1227724E/pt unknown
- 2000-10-10 WO PCT/EP2000/009929 patent/WO2001030155A2/fr not_active Ceased
- 2000-10-10 AT AT00967851T patent/ATE264057T1/de active
- 2000-10-10 CZ CZ20021461A patent/CZ300329B6/cs not_active IP Right Cessation
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- 2000-10-10 DE DE50006096T patent/DE50006096D1/de not_active Expired - Lifetime
- 2000-10-10 RS YUP-305/02A patent/RS50472B/sr unknown
- 2000-10-10 RU RU2002113744/04A patent/RU2266647C2/ru active
- 2000-10-10 UA UA2002054295A patent/UA72940C2/uk unknown
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- 2000-10-10 MX MXPA02004150A patent/MXPA02004150A/es active IP Right Grant
- 2000-10-10 CA CA002388909A patent/CA2388909C/fr not_active Expired - Lifetime
- 2000-10-10 CN CNB008159947A patent/CN1201658C/zh not_active Expired - Lifetime
- 2000-10-10 PL PL356696A patent/PL200935B1/pl unknown
- 2000-10-10 DK DK00967851T patent/DK1227724T3/da active
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- 2000-10-10 HR HR20020355A patent/HRP20020355B1/xx not_active IP Right Cessation
- 2000-10-10 BR BR0015018-5A patent/BR0015018A/pt not_active Application Discontinuation
- 2000-10-10 AU AU77869/00A patent/AU770910B2/en not_active Expired
- 2000-10-10 SK SK536-2002A patent/SK286660B6/sk not_active IP Right Cessation
- 2000-10-23 CO CO00080431A patent/CO5231160A1/es not_active Application Discontinuation
- 2000-10-24 AR ARP000105591A patent/AR026224A1/es active IP Right Grant
- 2000-10-24 MY MYPI20004991A patent/MY120861A/en unknown
- 2000-10-24 US US09/694,869 patent/US6569805B1/en not_active Expired - Lifetime
- 2000-10-24 TW TW089122362A patent/TWI243018B/zh not_active IP Right Cessation
2002
- 2002-04-23 ZA ZA200203207A patent/ZA200203207B/en unknown
2004
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Publication number	Publication date
SK5362002A3 (en)	2002-10-08
HUP0203119A3 (en)	2003-04-28
CO5231160A1 (es)	2002-12-27
CN1391440A (zh)	2003-01-15
BR0015018A (pt)	2002-06-18
JP2003512398A (ja)	2003-04-02
ATE264057T1 (de)	2004-04-15
CA2388909A1 (fr)	2001-05-03
EP1227724A2 (fr)	2002-08-07
AU770910B2 (en)	2004-03-04
TWI243018B (en)	2005-11-11
ES2219404T3 (es)	2004-12-01
MY120861A (en)	2005-11-30
WO2001030155A3 (fr)	2001-10-25
PL200935B1 (pl)	2009-02-27
HRP20020355A2 (en)	2004-02-29
MXPA02004150A (es)	2002-10-17
CZ20021461A3 (cs)	2002-09-11
AU7786900A (en)	2001-05-08
HRP20020355B1 (en)	2011-03-31
UA72940C2 (uk)	2005-05-16
YU30502A (sh)	2005-06-10
ZA200203207B (en)	2003-02-25
WO2001030155A2 (fr)	2001-05-03
RU2266647C2 (ru)	2005-12-27
DK1227724T3 (da)	2004-08-09
SK286660B6 (sk)	2009-03-05
HU226076B1 (en)	2008-04-28
CL2004001106A1 (es)	2005-04-29
CN1201658C (zh)	2005-05-18
PL356696A1 (en)	2004-06-28
RS50472B (sr)	2010-03-02
HUP0203119A2 (hu)	2003-01-28
PT1227724E (pt)	2004-09-30
EP1227724B1 (fr)	2004-04-14
US6569805B1 (en)	2003-05-27
AR026224A1 (es)	2003-01-29
DE50006096D1 (de)	2004-05-19
CA2388909C (fr)	2009-05-12

Legal Events

Date	Code	Title	Description
2020-10-21	MK4A	Patent expired	Effective date: 20201010

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AU2008243445B2 (en)	2013-10-03	Defoliant
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